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Association of MAPK4 and SOX1-OT gene polymorphisms with cleft lip palate in multiplex families: A genetic study

机译:MAPK4和SOX1-OT基因多态性与多重家族中唇腭裂的基因多态性:遗传学研究

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Background. Cleft lip and palate (CLP) is a common congenital anomaly. Many genes, like MAPK4 and SOX1-OT, are associated with its etiology in different populations. High-risk markers on these genes reported in other populations were not studied in our population. Hence, the study aimed to determine the association of MAPK4 and SOX1-OT polymorphisms in CLP in multiplex families. Methods. Based on inclusion and exclusion criteria, we selected 20 multiplex CLP families for this case?control study, in which the affected individuals and healthy controls selected from these families were compared. Fifty subjects affected with cleft and 38 unaffected subjects were included in the study. The polymorphisms studied for the association consisted of rs726455 and rs2969972 in the genes SOX1-OT and MAPK4, respectively. DNA was isolated and sent for genotyping using the MassArray method. Plink, a whole-genome association analysis toolset, was used for statistical analysis. Results. Both polymorphisms followed Hardy–Weinberg equilibrium. The rs726455 of SOX1-OT yielded a P-value of 0.983 and an allelic odds ratio (OR) of 0.983. For rs2969972 of MAPK4, the P-value was 0.04 (significant), and the allelic OR was 0.51. Minor allele frequency (MAF) in the unaffected subjects was more than the MAF in the affected subjects for rs2969972. Conclusion. The results suggested that polymorphism rs726455 on SOX1-OT was not associated with familial cases of CLP. Since MAF in the unaffected subjects was more than the MAF-affected subjects, rs2969972 on MAPK4 is protective in the multiplex families.
机译:背景。裂隙唇和口感(CLP)是一个常见的先天性异常。许多基因,如MAPK4和SOX1-OT,与其在不同群体中的病因相关联。在其他人群中报道的这些基因上的高风险标志物未在我们的人口中进行。因此,该研究旨在确定MAPK4和SOX1-OT多态性在多路复用家族中CLP中的关联。方法。基于包含和排除标准,我们为这种情况选择了20个多路复用CLP系列?对照研究,其中比较了从这些家庭中选择的受影响的个体和健康对照。研究中包含50个受试者和38个未受影响的受试者的受试者。所研究的多态性分别在基因SOX1-OT和MAPK4中分别由RS726455和RS2969972组成。分离DNA并使用MassArray方法送去用于基因分型。 Plink是一个全基因组关联分析工具集用于统计分析。结果。两种多态性遵循Hardy-Weinberg均衡。 SOx1-OT的RS726455产生0.983的p值,等位基因差值(或)为0.983。对于MAPK4的RS2969972,P值为0.04(显着),等位基因或0.51。未受影响的受试者的次要等位基因频率(MAF)超过受影响受试者的MAF,适用于RS2969972。结论。结果表明,SOX1-OT上的多态性RS726455与CLP的家族病例无关。由于未受影响的受试者的MAF超过MAF受影响的受试者,MAPK4上的RS2969972在多路复用家庭中是保护的。

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